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Supply Chain Senior Associate
Company | Aequor |
Address | United States |
Employment type | CONTRACTOR |
Salary | |
Category | Medical Equipment Manufacturing,Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-09-22 |
Posted at | 8 months ago |
Job Title: MCS Supply chain Senior Associate
Location: Remote
Description:
REMOTE
Standard business hours
Supply Chain Sr. Associate - External Planning & Delivery
Overview:
The EPD team manages the forecast planning and supply chain activities for several contract manufacturing sites. The role of the EPD team through consultation with Contract Manufacturing site managers and global product planners, manage material requirements planning, ordering and payment, CMO batch management from planning to distribution and CMO performance management through agreed KPI’s and Metrics.
Key Responsibilities May Include But Not Limited To:
EPD Planner
• Responsible for the coordination of logistics activities, regular interface with internal and external clients, and issue resolution.
o Coordination of outgoing shipments from CMO to specific Sites or contract labs
• Participate in weekly team calls with CMO’s.
• Monitor batch tracking and EPD activities required to meet supply within contract timelines
• Assist with managing progress of orders through SAP transactions for full manufacturing and logistic process
• Material requirements planning for CMO’s including ordering, invoice payment and expiry management
• Maintain current purchase orders and master data in SAP using current procurement information
• Participate as needed in the monthly Planning Cycle for CMO forecast generation
o Use of SAP to place orders as required.
o Send forecasts to CMO’s and manage changes, negotiations, and communications.
Minimum Requirements
• 1+ years’ Supply Chain experience in GMP environment
• 1+ years’ SAP experience (Plan-to-Stock, inventory management)
• Experience in using SAP, Excel and MS Office Fluent
Preferred Requirements:
• Bachelor’s degree or equivalent
• Typically 3+ years of related professional experience.
• Knowledge of cGMP and other regulatory requirements are required
• Excellent organization and problem-solving skills
• Very good interpersonal skills: ability to interact with multiple stakeholders in an organization
• Ability to communicate findings and make recommendation to the wider organization
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